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TerminatedNCT00215098Updated Mar 16, 2012

Chylothorax Following Heart Surgery

An observational study in Chylothorax, sponsored by Children's Healthcare of Atlanta. Terminated at 1 site in United States. Per ClinicalTrials.gov, last updated 2012-03-16.

Sponsored by Children's Healthcare of Atlanta · Observational

Why this study was terminated
insufficient data
Study type
Observational
Time perspective
Retrospective
Enrollment
70
Sex
All
01

Study summary

The purpose of this study is to determine at risk populations for certain congenital heart defects or certain operative procedures and to define the associated morbidity secondary to chylothorax - prolonged chest tube drainage, prolonged hospital stay, need for central access and hyperalimentation, subsequent infection.

Read the detailed description

Chylothorax is not uncommon following congenital heart surgery. It often results in prolonged chest tube drainage and hospital stays. Due to the feeding difficulties, it often results in malnutrition and the need for central hyperalimentation. In addition, it results in a depressed immune system with the possibility of subsequent infection. Chylothorax can be a significant contributor to post-operative morbidity and mortality.

The primary aims are to determine at risk populations - certain congenital heart defects or certain operative procedures, to define the associated morbidity secondary to chylothorax - prolonged chest tube drainage, prolonged hospital stay, need for central access and hyperalimentation, subsequent infection and to review our current treatment methods - change formulas, hyperalimentation, somatostatin. The secondary aims are to determine ways to prevent chylothorax, determine the most successful treatment method, and to discover better treatment methods. This study will be conducted through a retrospective chart review.

02

Conditions studied

  • Chylothorax

Keywords

  • pediatric health
  • cardiac
  • congenital heart surgery
  • post-operative chylous effusions
  • heart defects
  • children
03

In context

Lead sponsor

Children's Healthcare of Atlanta is the lead sponsor of 95 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients in the congenital surgery database

Inclusion criteria

  • Patients in the congenital surgery database
  • patients have developed post-operative chylous effusions

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Time perspective
Retrospective
Enrollment
70 participants (estimated)
06

Study locations

1 site
  • Children's Healthcare of Atlanta at Egleston
    Atlanta, Georgia 30322, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 16, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00215098
Lead sponsor
Children's Healthcare of Atlanta
First posted
Sep 22, 2005
Start date
May 2005
Completion
Nov 2006
Last update
Mar 16, 2012

Study contacts

Brian Kogon, MD
principal investigator · Emory University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Jun 2007. You cannot join it, but the record below documents what was studied.

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